Canonical Allele Identifier: CA564088973
Gene:

Linked Data

dbSNP Id: rs1174413613
gnomAD v2: 5-159007893-A-G
MyVariant Identifiers: chr5:g.159007893A>G (hg19) chr5:g.159580885A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.159580885A>G , CM000667.2:g.159580885A>G GRCh38
NC_000005.9:g.159007893A>G , CM000667.1:g.159007893A>G GRCh37
NC_000005.8:g.158940471A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_941139.1:n.2075+450A>G
XR_941140.1:n.2075+450A>G
XR_941141.1:n.570+450A>G
XR_941139.2:n.2229+450A>G
Search 100 bp 5'
Search 100 bp 3'